|Publication number||US3970717 A|
|Application number||US 05/522,399|
|Publication date||Jul 20, 1976|
|Filing date||Nov 11, 1974|
|Priority date||Nov 9, 1973|
|Also published as||DE2355942A1, DE2355942B1|
|Publication number||05522399, 522399, US 3970717 A, US 3970717A, US-A-3970717, US3970717 A, US3970717A|
|Inventors||Horst Muller-Albrecht, Bernd Quiring, Manfred Dollhausen, Jochen Wulff|
|Original Assignee||Bayer Aktiengesellschaft|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (27), Classifications (23)|
|External Links: USPTO, USPTO Assignment, Espacenet|
It is known that adhesives suitable for bonding a wide variety of materials such as leather, synthetic leather, rubber or plastics can be prepared from high-molecular weight hydroxy-polyurethanes. Adhesives of this kind have been described, inter alia, in German Pat. No. 1,256,822.
If such adhesives are applied without heating ("cold sealing process"), a sufficiently strong bond, especially immediately after glueing ("instant strength"), is obtained only if bonding is carried out within a certain interval of time ("open time"). For the majority of adhesives applied in this way, this "open time" is extremely brief, i.e. only a few minutes. Faulty bonds are obtained not only if the open time is exceeded but also if a shorter time is used. In order to avoid this, the adhesives are applied by a thermal activating process in which the layers of adhesive are heated to about 80°C (i.e. activated), e.g., by infrared irradiation, before they are joined together. This thermal activation process, however, cannot always be applied. It firstly requires considerable expenditure relative to the apparatus to be used. Moreover, many materials, e.g. plastic sheets, are subject to deformation or damage by such treatment.
Investigations have been carried out with the object of overcoming these serious disadvantages by increasing the "open time" of hydroxy-polyurethane adhesives by means of addition of various kinds of resins. The adhesives with longer "open times" obtained in this way, however, gave rise to bonds which were not strong enough for many purposes, particularly immediately after bonding ("instant strength"). Furthermore, the addition of resins also reduced the adherence of the adhesives to many materials and substantially reduced the resistance of the bonds to plasticizers.
It has now surprisingly been found that adhesives which have very long "open times" and which produce bonds which combine previously unattained "instant strength" with rapid setting can be prepared from certain high-molecular weight hydroxy polyurethanes and styrene copolymers. The resistance of the bonds to plasticizers is excellent. Moreover, bonds produced using the adhesives according to the instant invention have greater resistance to moist, hot atmospheres. In addition, the layers of adhesive undergo substantially less yellowing when they are exposed to light, e.g. in transparent composite foils.
This invention, therefore, relates to compositions suitable for use as adhesives comprising;
A. an hydroxy polyester urethane having a molecular weight above about 30,000 and
B. a polymer selected from the group consisting of (1) copolymers of styrene and/or α-methyl styrene with at least one other olefinically unsaturated monomer and (2) mixtures of (1) with rubbery elastic polymers.
The invention also relates to compositions particularly suitable for this use, comprising;
A. a hydroxy polyesterurethane having a molecular weight above 30,000 derived from
1. a polyester with a molecular weight above about 600 selected from the group consisting of
a. adipic acid and butane-1,4-diol and/or hexane-1,6-diol polyesters,
b. ε-polycaprolactone and,
c. dihydroxy polyhexamethylene carbonate;
2. from 0 to 400 mol percent, based on the polyester (1), of a diol chain-lengthening agent having a molecular weight of between about 62 and about 300, and,
3. an organic polyisocyanate; and
B. a polymer selected from the group consisting of;
1. a thermoplastic copolymer of styrene and/or α-methyl styrene with acrylonitrile, said copolymer containing from about 40 to about 80 percent by weight of styrene and/or α-methyl styrene and
2. a mixture of
a. from about 5 to about 60 percent by weight of a graft polymer obtained by grafting an acrylonitrile/styrene and/or acrylonitrile/α-methyl styrene mixture on polybutadiene, and which contains from about 30 to about 70 percent by weight of butadiene units from about 5 to about 20 percent by weight of acrylonitrile units and from about 25 to about 50 percent by weight of styrene and/or α-methyl styrene units and
b. from about 95 to about 40 percent by weight of the copolymer mentioned under (1)
the weight ratio of A:B preferably being between 1:0.05 and 1:3.
Component A of the compositions according to the instant invention consists of substantially linear hydroxy polyester urethanes which have molecular weights determined by the scattered light method of more than 30,000 and preferably between 50,000 and 1,000,000. Preparation of such hydroxy polyester urethanes is carried out in known manner by reacting dihydroxy polyesters which have a molecular weight above 600 and preferably between 2000 and 4000 with subequivalent quantities of polyisocyanate, to which low-molecular weight difunctional chain-lengthening agents may be added.
Suitable dihydroxy polyesters are, in particular, those derived from saturated dicarboxylic acids which preferably contain at least 6 carbon atoms and saturated diols which preferably contain at least 4 carbon atoms. Suitable dicarboxylic acids are, for example, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid and the like. Suitable diols are, for example, butane-1,4-diol, pentane-1,5-diol, hexane-1,6-diol, and the like. Apart from such polyesters, hydroxy polycarbonates, in particular those of hexane-1,6-diol and diaryl carbonates, as well as esterification products of straight chain hydroxy alkane monocarboxylic acids which contain at least 5 carbon atoms or the corresponding lactone polymers may also be used.
Hydroxy polyesters of adipic acid and butane-1,4-diol and of adipic acid and hexane-1,6-diol and hydroxy polyesters of ε-caprolactone and hexane-1,6-diol polycarbonates with hydroxyl end groups are presently preferred. The polyesters used preferably have molecular weights of 2000 to 4000.
Essentially any organic polyisocyanate may be used. However, it is preferred to use aliphatic, cycloaliphatic, araliphatic and aromatic diisocyanates, e.g. butane-1,4-diisocyanate, hexane-1,6-diisocyanate, cyclohexane-1,4-diisocyanate, 1-methyl-2,4-diisocyanatocyclohexane, 1-methyl-2,6-diisocyanato-cyclohexane, 1-isocyanato-3-isocyanatomethyl-3,5,5-trimethylcyclohexane, 2,4- and -2,6-diisocyanatotoluene, 4,4'-diphenylmethane-diisocyanate, 4,4-diphenylpropane-diisocyanate or mixtures of such diisocyanates, 4,4'-diphenylmethane diisocyanate and 2,4- and -2,6-diisocyanatotoluene and mixtures thereof.
Suitable chain-lengthening agents, which are optional, are in particular, diols having a molecular weight of between about 62 and about 300 e.g. esterdiols, such as terephthalic acid-bis-2-hydroxyethylester, or etherdiols, such as hydroquinone-bis-2-hydroxyethylether, but aliphatic diols such as ethylene glycol, propane-1,3-diol, butane-1,4-diol, pentane-1,5-diol, hexane-1,6-diol and the like are generally preferred.
The diols may also be used as mixtures. The total quantities in which they are used are from 0 to 400 mol percent preferably from 0 to 200 mol percent, based on the hydroxy polyester.
Component B of the compositions according to the instant invention are preferably
a. thermoplastic copolymers of styrene and/or α-methyl styrene with at least one other olefinically unsaturated monomer, which copolymers have a softening point about 70°C determined according to DIN 53,460 and contain 60-20 percent by weight of units corresponding to other olefinically unsaturated monomers in addition to 40-80 percent by weight of styrene and/or α-methyl styrene units, or
b. mixtures of copolymers (a) with rubbery elastic polymers, the said mixtures preferably containing components (a) and rubbery elastic polymers in proportions by weight of between 40:60 and 95:5.
The thermoplastic copolymers (a) are copolymers of styrene and/or α-methyl styrene with at least one other olefinically unsaturated monomer such as acrylonitrile, methacrylonitrile, methylacrylate or methyl methacrylate. Component (a) is preferably a copolymer of styrene and/or α-methyl styrene, and acrylonitrile.
Component (b) which may, if desired, be used instead of the pure component (a) consists of mixtures of component (a) with rubbery elastic polymers which have a freezing temperature of below 20°C determined according to DIN 53,513. Suitable examples are, in particular, graft polymers obtained by grafting a styrene/acrylonitrile and/or an α-methyl styrene/acrylonitrile mixture on polybutadiene, for example, in accordance with U.S. Pat. No. 2,820,773. Particularly suitable graft polymers contain from about 30 to about 70 percent by weight of butadiene units, from about 5 to about 20 percent by weight of acrylonitrile units and from about 25 to about 50 percent by weight of styrene and/or α-methyl styrene units.
Instead of the above-mentioned graft polymers, however, there may, of course, be used graft polymers in which the butadiene has been partly or completely replaced by isoprene or the acrylonitrile has been partly or completely replaced by methacrylonitrile and/or C1 -C18 alkyl esters of acrylic or methacrylic acid. As recognized in the art, the graft polymers may be prepared by solution, suspension, precipitation or mass polymerization processes. One particularly suitable process for preparing graft polymers of the type presently contemplated has been described in U.S. Pat. No. 2,820,773.
Component (b), may in principle, contain any other rubbery elastic polymer with a freezing temperature of below 20°C (DIN 53,513) instead of the above-mentioned preferred graft polymers. Suitable rubbery elastic polymers are, for example, rubbery elastic polyacrylic acid esters, EPDM rubbers and polyalkenamer rubbers. These rubbery elastic polymers used for rubber modification of component (a) may be prepared in known manners by solution of emulsion processes.
Rubber modification of the thermoplastic copolymer (a) may be carried out by mixing the copolymer with the rubbery elastic polymer and thermoplastic copolymer in a manner similar to Example IV of U.S. Pat. No. 2,820,773.
Component B may also consist exclusively of graft polymers of the type described.
In the compositions according to the instant invention, components A and B are preferably present in weight ratios of between 1:0.05 and 1:3 and preferably between 1:0.2 and 1:1.5.
These compositions are preferably prepared by mixing the components preferably under conditions of homogenization on rollers, extruder screws or other suitable machines.
The resulting compositions yield viscous adhesives when mixed with solvents such as ethyl acetate, acetone or methyl ethyl ketone. These adhesives may also be prepared by stirring the component (B) into a hydroxy polyester polyurethane solution. The compositions are generally used as 10% to 40% solutions. As recognized in the art, the adhesives may be modified e.g. by adding polyisocyanates, catalysts, natural or synthetic resins, organic acids, fillers and the like.
The adhesives are used by applying them to the surfaces which are to be bonded together, if necessary, after first rubbing down the surfaces to roughen them or preparing them in some other manner. The adhesives may be applied by rollers, brushes, spatulas, spray guns or some other device. The adhesive when applied is left to dry and the materials coated with the adhesive are then pressed together within the "open time".
The adhesives according to the invention can be used for obtaining firm bonds with various materials such as paper, cardboard, wood, metal, or leather. They are preferably used for bonding rubber materials and in particular, synthetic resins including polyurethane foams which have a compact surface plasticizer-containing homopolymers or copolymers of vinyl chloride, and above all, for bonding shoe soles made of these materials to shoe uppers made of leather or synthetic leather.
The adhesives were prepared by stirring the compositions according to the invention into methyl ethyl ketone.
Table 1 shows the compositions of the binders used.
Table 2 shows the compositions of the polyurethanes used.
Table 3 shows the compositions of the polymers.
Bonds were produced with the adhesives. The following materials were bonded:
a. A commercial rubber material, 4 mm thick, made of acrylonitrile butadiene rubber (acrylonitrile content 33%, Defo hardness 700 according to DIN 53,514) which contained about 31% of silicate filler (Shore hardness A of rubber material 85 according to DIN 53,505) and
b. A PVC material, 4 mm thick, made of 70 parts by weight of polyvinyl chloride (K-value 80), 30 parts by weight of dioctyl phthalate as plasticizer and 5 parts by weight of epoxydized soya-bean oil and 1.2 parts by weight of barium-cadmium laurate.
Before the adhesives were applied, the surfaces of sample strips of materials 15 cm in length and 3 cm in width which were to be bonded were thoroughly rubbed down with a grade 40 sanding belt. The materials were freed from sanding dust and coated with the individual adhesives and then kept open at room temperature and joined together after the times indicated in Table 4 and pressed together for 15 seconds under a pressure of 3 kg/cm2. The resistance to separation was tested according to DIN 53,274 immediately after the materials had been bonded and 1 day and 9 days later. The resistance to separation are also shown in Table 4.
Table 1______________________________________Adhesive* Polyurethane A Polymer B A : B______________________________________1 (comparison) I -- 1 : 02 I I 1 : 13 I II 1 : 0.54 I II 1 : 15 I III 1 : 16* (comparison) I -- 1 : 07* I II 1 : 18 (comparison) II -- 1 : 09 II II 1 : 0.510 (comparison) III -- 1 : 011 III II 1 : 112 I IV 1 : 1______________________________________ *10% of a 20% solution of 4,4',4"-triisocyanato-triphenylmethane in methylene chloride were added to the 20% adhesive.
TABLE 2__________________________________________________________________________Polyurethane Polyester Polyisocyanate Chain-lengthening__________________________________________________________________________ agentI 1000 g of adipic acid/ 81.2 g of isomeric -- butane-1,4-diol mixture (80:20) polyester with of 2,4- and 2,6- OH-number 52.4 diisocyanato- tolueneII 1000 g of adipic acid/ 163.5 g of 4,4'-diiso- 16.8 g of butane 1,4- butane-1,4-diol cyanato-diphenyl- diol polyester with methane OH-number 52.4II 1000 g of poly-ε-capro- 58.6 g of isomeric lactone with OH- mixture (80:20) number 37.9 of 2,4- and -2,6- diisocyanato- toluene__________________________________________________________________________
Table 3__________________________________________________________________________Polymer*Copolymer (a) of Graft polymer (b) of Ratio of (a) : (b)styrene acrylonitrile styrene acrylonitrile butadiene(% by weight) (% by weight) (% by weight) (% by weight) (% by weight)__________________________________________________________________________I 72 28 -- -- -- --II 72 28 36 14 50 3 : 1III 72 28 36 14 50 65 : 35IV -- -- 36 14 50 --__________________________________________________________________________ *Polymer I is a pure polymer while polymers II and III are mixtures of this copolymer with the given graft polymer. The copolymer was prepared b emulsion polymerization. Mixtures II and III were prepared in a manner similar to Example IV of U.S. Patent Specification No. 2,820,773. Graft polymer IV was also prepared in a manner similar to the method described in U.S. Patent Specification No. 2,820,773.
Table 4__________________________________________________________________________ Resistance to separation (kp/cm)Adhesive Bonds joined together Rubber Rubber Soft PVC Soft PVC after minutes immediately 1 day 9 days immediately 1 day 9 days__________________________________________________________________________1 (compar- ison) 15 <0.1 <0.1 <0.1 <0.1 <0.1 <0.12 240 0.9 3.1 3.6 1.1 4.6 5.93 120 1.1 2.9 3.7 1.3 4.6 7.04 240 1.6 2.7 3.6 1.3 4.7 7.15 240 0.8 3.3 3.5 0.8 5.2 6.26* (compar- ison) 15 <0.1 <0.1 <0.1 <0.1 <0.1 <0.17* 120 0.8 3.2 3.8 0.9 5.3 9.58 (compar- ison) 15 <0.1 <0.1 <0.1 <0.1 <0.1 <0.19 120 0.5 2.7 3.3 0.5 4.3 5.210 (compar- ison) 60 <0.1 <0.1 <0.1 <0.1 <0.1 <0.111 120 0.4 2.9 3.5 0.5 3.2 5.312 120 0.5 2.2 2.8 0.5 2.8 3.6__________________________________________________________________________
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3358052 *||May 4, 1964||Dec 12, 1967||Mobay Chemical Corp||Polyurethane composition containing 0.2 to 5% polyolefin or polystyrene|
|US3368988 *||Apr 9, 1963||Feb 13, 1968||Desoto Inc||Solvent-soluble, non-gelled interpolymer comprising resinous hydroxy-terminated polyethylenically unsaturated polyurethane|
|US3385909 *||Jan 12, 1965||May 28, 1968||Mobay Chemical Corp||Polyurethane resins blended with poly-lower alkyl styrene resins|
|US3457324 *||Jun 10, 1966||Jul 22, 1969||Desoto Inc||Thermosetting coating compositions comprising hydroxy-functional interpolymers|
|US3597495 *||Jul 1, 1968||Aug 3, 1971||Desoto Inc||Thermosetting coatings comprising hydroxy-functional polyurethane interpolymers|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4049590 *||Nov 24, 1975||Sep 20, 1977||Basf Aktiengesellschaft||Manufacture of polyurethane compositions|
|US4101473 *||Jan 15, 1976||Jul 18, 1978||Story Chemical Corporation||Solid particle-form polymerizable polymeric material and compositions, structures and methods of employing and producing the same|
|US4145511 *||Sep 1, 1977||Mar 20, 1979||The B. F. Goodrich Company||Hydroxyl-containing liquid polymers and pressure-sensitive adhesives and laminates prepared therefrom|
|US4145514 *||Sep 1, 1977||Mar 20, 1979||The B. F. Goodrich Company||Polyurethane pressure-sensitive adhesive and laminates therefrom|
|US4172060 *||May 25, 1977||Oct 23, 1979||Hoechst Aktiengesellschaft||Reactive lacquer composition based on unsaturated polyesters|
|US4251642 *||Aug 15, 1979||Feb 17, 1981||Borg-Warner Corporation||Compatible polyurethane blends|
|US4317890 *||Dec 13, 1979||Mar 2, 1982||Bayer Aktiengesellschaft||Thermoplastic synthetic material and a process for its production|
|US4342847 *||Dec 13, 1979||Aug 3, 1982||Bayer Aktiengesellschaft||Process for the production of thermoplastic synthetic materials|
|US4500671 *||Jun 1, 1984||Feb 19, 1985||Bayer Aktiengesellschaft||Reinforced polyurethane thermoplastic chemical materials and processes for their preparation|
|US4539366 *||Feb 22, 1984||Sep 3, 1985||Rhone-Poulenc Specialites Chimiques||Sizing composition and method of making same and use thereof for sizing textile yarns|
|US4551382 *||Jan 25, 1985||Nov 5, 1985||Rhone-Poulenc Specialites Chimiques||Sizing composition and method of making same and use thereof for sizing textile yarns|
|US4585819 *||Aug 14, 1984||Apr 29, 1986||H. B. Fuller Company||Fusion adhesive which can comprise an isocyanate prepolymer, a thermoplastic polymer and/or a lower molecular weight ketone resin|
|US4775719 *||Jan 29, 1986||Oct 4, 1988||H. B. Fuller Company||Thermally stable hot melt moisture-cure polyurethane adhesive composition|
|US4808255 *||May 7, 1987||Feb 28, 1989||H. B. Fuller Company||Thermally stable reactive hot melt urethane adhesive composition having a thermoplastic polymer, a compatible, curing urethane polyester polyol prepolymer and a tackifying agent|
|US4820368 *||May 7, 1987||Apr 11, 1989||H. B. Fuller Company||Thermally stable reactive hot melt urethane adhesive composition having a thermoplastic polymer, a compatible, curing urethane polyalkylene polyol prepolymer and a tackifying agent|
|US4891269 *||Mar 7, 1988||Jan 2, 1990||H. B. Fuller Company||Bonding method employing thermally stable hot melt moisture-cure polyurethane adhesive composition|
|US4913971 *||Apr 27, 1989||Apr 3, 1990||Bayer Aktiengesellschaft||Adhesive mixture|
|US4980417 *||Jun 26, 1989||Dec 25, 1990||Montedipe S.P.A.||Polymeric blends based on vinyl-aromatic polymers|
|US5055525 *||Feb 23, 1990||Oct 8, 1991||The Dow Chemical Company||Low temperature toughened thermoplastic polymer blend compositions|
|US5194494 *||Feb 23, 1990||Mar 16, 1993||The Dow Chemical Company||Heat resistant thermoplastic polymer blends|
|US5216062 *||Jul 30, 1992||Jun 1, 1993||Basf Aktiengesellschaft||Thermoplastic polyurethane molding composition|
|US5225476 *||Sep 16, 1991||Jul 6, 1993||The B. F. Goodrich Company||Fiber-reinforced thermoplastic molding composition|
|US5258445 *||Mar 6, 1992||Nov 2, 1993||The B. F. Goodrich Company||Fiber-reinforced thermoplastic molding compositions using a copolyester|
|US5260375 *||Feb 25, 1991||Nov 9, 1993||Basf Aktiengesellschaft||Thermoplastic moldings materials of improved green strength and low-temperature toughness based on a thermoplastics polyurethane copolymer mixture, preparation thereof and use thereof|
|US5334647 *||Jul 1, 1993||Aug 2, 1994||The B. F. Goodrich Company||Fiber-reinforced thermoplastic molding compositions|
|US5519094 *||Oct 29, 1993||May 21, 1996||B. F. Goodrich Company||Fiber-reinforced thermoplastic molding compositions using a modified thermoplastic polyurethane|
|US6540704 *||Jun 23, 1999||Apr 1, 2003||Bsn Medical Gmbh & Co. Kg||Orthopedic bandage|
|U.S. Classification||525/66, 525/125, 528/74.5, 521/137, 528/80, 525/67, 528/83, 525/130|
|International Classification||C08L25/12, C08L75/06, C08L51/04, C09J175/06, C08L25/02|
|Cooperative Classification||C08L25/02, C09J175/06, C08L75/06, C08L51/04, C08L25/12|
|European Classification||C08L51/04, C08L25/02, C08L75/06, C08L25/12, C09J175/06|